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1.
Org Lett ; 7(8): 1489-91, 2005 Apr 14.
Article in English | MEDLINE | ID: mdl-15816734

ABSTRACT

[reaction: see text] Pauson-Khand cyclization of dioxanone photoadduct 21 leads to the formation of a single product in good yield. However, retro-aldol fragmentation of the pentacyclic cyclopentenone 22 leads to the formation of 23, with cis C-8/C-10 intrabridgehead stereochemistry, unlike the target compound ingenol 1, which possesses C-8/C-10 trans intrabridgehead stereochemistry.


Subject(s)
Diterpenes/chemical synthesis , Cyclization , Diterpenes/chemistry , Molecular Structure , Stereoisomerism
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